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4-Aminomethyl-4-fluoro-piperidine-1-carboxylic acid tert-butyl ester, also known as tert-Butyl 4-(aminomethyl)-4-fluoropiperidine-1-carboxylate, is a chemical compound that serves as a crucial intermediate in the synthesis of 4-aminomethyl-4-fluoropiperidine derivatives. These derivatives are known for their ability to act as T-type Ca2+ channel antagonists, which are significant in various medical applications.
Used in Pharmaceutical Industry:
4-Aminomethyl-4-fluoro-piperidine-1-carboxylic acid tert-butyl ester is used as a key intermediate in the synthesis of T-type Ca2+ channel antagonists for the development of medications targeting specific therapeutic areas. The T-type Ca2+ channel antagonists derived from this compound have potential applications in treating various conditions, such as neuropathic pain, certain types of epilepsy, and other neurological disorders, due to their ability to modulate calcium channel activity.

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    Cas No: 620611-27-0

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    Cas No: 620611-27-0

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  • 620611-27-0 Structure
  • Basic information

    1. Product Name: 4-Aminomethyl-4-fluoro-piperidine-1-carboxylic acid tert-butyl ester
    2. Synonyms: 4-Aminomethyl-4-fluoro-piperidine-1-carboxylic acid tert-butyl ester;1-PIPERIDINECARBOXYLIC ACID, 4-(AMINOMETHYL)-4-FLUORO-, 1,1-DIMETHYLETHYL ESTER;TERT-BUTYL 4-(AMINOMETHYL)-4-FLUOROPIPERIDINE-1-CARBOXYLATE;1-Boc-4-(aMinoMethyl)-4-fluoropiperidine;1-Boc-4-(aMinoMethyl)-4-f...;1-Boc-4-fluoro-4-(aMinoMethyl)-piperidine;4-Aminomethyl-4-fluoro-piperidine-1-carboxylic acid tert-butyl ester PUIRTY:>95%
    3. CAS NO:620611-27-0
    4. Molecular Formula: C11H21FN2O2
    5. Molecular Weight: 232.297
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 620611-27-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 302.4 °C at 760 mmHg
    3. Flash Point: 136.7 °C
    4. Appearance: /
    5. Density: 1.09 g/cm3
    6. Refractive Index: 1.483
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    8. Solubility: N/A
    9. PKA: 10.13±0.29(Predicted)
    10. CAS DataBase Reference: 4-Aminomethyl-4-fluoro-piperidine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-Aminomethyl-4-fluoro-piperidine-1-carboxylic acid tert-butyl ester(620611-27-0)
    12. EPA Substance Registry System: 4-Aminomethyl-4-fluoro-piperidine-1-carboxylic acid tert-butyl ester(620611-27-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 620611-27-0(Hazardous Substances Data)

620611-27-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 620611-27-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,0,6,1 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 620611-27:
(8*6)+(7*2)+(6*0)+(5*6)+(4*1)+(3*1)+(2*2)+(1*7)=110
110 % 10 = 0
So 620611-27-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H21FN2O2/c1-10(2,3)16-9(15)14-6-4-11(12,8-13)5-7-14/h4-8,13H2,1-3H3

620611-27-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-(aminomethyl)-4-fluoropiperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 4-(aminomethyl)-4-fluoropiperidine-1-ncarboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:620611-27-0 SDS

620611-27-0Relevant articles and documents

AMIDE COMPOUNDS AS 5-HT4 RECEPTOR AGONISTS

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Page/Page column 36, (2016/09/22)

The present invention relates to compounds of formula (I), including their stereoisomers and pharmaceutically acceptable salts. This invention also relates to methods of making such compounds and pharmaceutical compositions comprising such compounds. The compounds of this invention are useful in the treatment of various disorders that are related to 5-hydroxytryptamine 4 (5-HT4) receptor.

INDAZOLE COMPOUNDS AS 5-HT4 RECEPTOR AGONISTS

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Page/Page column 28, (2015/07/07)

The present invention relates to novel indazole compounds of the Formula (I), wherein, R1 is alkyl or cycloalkyl; (Formula II) including their stereoisomers and their pharmaceutically acceptable salts. This invention also relates to methods of making such compounds and pharmaceutical compositions comprising such compounds. The compounds of this invention are useful in the treatment of various disorders that are related to 5-Hydroxytryptamine 4 (5-HT4) receptor agonists

5-AMINO-QUINOLINE-8-CARBOXAMIDE DERIVATIVES AS 5-HT4 RECEPTOR AGONISTS

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Page/Page column 33, (2014/10/03)

The present invention relates to novel quinoline compounds of formula (I), and their pharmaceutically acceptable salts and process for their preparation. The compounds of formula (I) are useful in the treatment of various disorders that are related to 5-HT4 receptor agonists.

Novel Compounds for the Treatment of Diseases Associated with Amyloid or Amyloid-like Proteins

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Page/Page column 20, (2011/10/31)

The present invention relates to novel compounds that can be employed in the treatment of a group of disorders and abnormalities associated with amyloid protein, such as Alzheimer's disease, and of diseases or conditions associated with amyloid-like prote

Novel compounds for the treatment of diseases associated with amyloid or amyloid-like proteins

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Page/Page column 27, (2011/11/01)

The present invention relates to novel compounds that can be employed in the treatment of a group of disorders and abnormalities associated with amyloid protein, such as Alzheimer's disease, and of diseases or conditions associated with amyloid-like prote

Synthesis of aminomethylated 4-fluoropiperidines and 3-fluoropyrrolidines

Verniest, Guido,Piron, Karel,Van Hende, Eva,Thuring, Jan Willem,MacDonald, Gregor,Deroose, Frederik,De Kimpe, Norbert

supporting information; experimental part, p. 2509 - 2512 (2010/07/05)

A short and efficient synthesis of 4-aminomethyl-4-fluoropiperidines and 3-aminomethyl-3-fluoropyrrolidines is described. These fluorinated azaheterocycles are of specific interest as bifunctional building blocks for fluorinated pharmaceutical compounds.

Design, synthesis, and evaluation of a novel 4-aminomethyl-4- fluoropiperidine as a T-type Ca2+ channel antagonist

Shipe, William D.,Barrow, James C.,Yang, Zhi-Qiang,Lindsley, Craig W.,Yang, F. Vivien,Schlegel, Kelly-Ann S.,Shu, Youheng,Rittle, Kenneth E.,Bock, Mark G.,Hartman, George D.,Tang, Cuyue,Ballard, Jeanine E.,Kuo, Yuhsin,Adarayan, Emily D.,Prueksaritanont, Thomayant,Zrada, Matthew M.,Uebele, Victor N.,Nuss, Cindy E.,Connolly, Thomas M.,Doran, Scott M.,Fox, Steven V.,Kraus, Richard L.,Marino, Michael J.,Graufelds, Valerie Kuzmick,Vargas, Hugo M.,Bunting, Patricia B.,Hasbun-Manning, Martha,Evans, Rose M.,Koblan, Kenneth S.,Renger, John J.

supporting information; scheme or table, p. 3692 - 3695 (2009/04/07)

The novel T-type antagonist (S)-5 has been prepared and evaluated in in vitro and in vivo assays for T-type calcium ion channel activity. Structural modification of the piperidine leads 1 and 2 afforded the fluorinated piperidine (S)-5, a potent and selec

4-FLUORO-PIPERIDINE T-TYPE CALCIUM CHANNEL ANTAGONISTS

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Page/Page column 23-24, (2010/11/25)

The present invention is directed to 4-fluoro-piperidine compounds which are antagonists of T-type calcium channels, and which are useful in the treatment or prevention of neurological and psychiatric disorders and diseases in which T-type calcium channel

4,4-DISUBSTITUTED PIPERIDINE DERIVATIVES HAVING CCR3 ANTAGONISM

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Page/Page column 369, (2008/06/13)

The invention provides low molecular compounds having activity which inhibits binding of CCR3 ligands to CCR3 on target cells, i.e. CCR3 antagonists. The invention also provides 4,4-(disubstituted)piperidine derivatives represented by formula (I) below, pharmaceutically acceptable acid adducts thereof, or pharmaceutically acceptable C1-C6 alkyl adducts thereof, as well as pharmaceutical compositions comprising them as effective ingredients, which are useful for treatment or prevention of diseases associated with CCR3, such as asthma and allergic rhinitis.

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